Align PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized)
to candidate WP_038857764.1 AFK65_RS05470 PTS transporter subunit EIIC
Query= SwissProt::Q57071 (675 letters) >NCBI__GCF_001277175.1:WP_038857764.1 Length = 499 Score = 454 bits (1167), Expect = e-132 Identities = 237/512 (46%), Positives = 327/512 (63%), Gaps = 33/512 (6%) Query: 4 KFFGQLQRIGKALMLPVAILPAAGLLLALGNAFQGDALQSLMPFIKAEGFQNVAKMMEGA 63 K +L IG+ALMLP+++LPAAGLLLA G+ F +M A Sbjct: 9 KSLSKLSMIGRALMLPISLLPAAGLLLAFGDKFH-------------------LPLMMNA 49 Query: 64 GGIIFDNLAIIFALGVAIGLASGDGVAAIAAFVGFIVLNKTMGMFLGVTPEKAADAATGF 123 GG+IFDNL ++FA+G A+GLAS G+AA++A V ++N T+ LG+TPE AA + Sbjct: 50 GGVIFDNLPLLFAIGSAVGLASESGIAALSAAVSVFIINITISTQLGITPEMAASGGK-Y 108 Query: 124 ANVLGIPTLQTGVFGGIIIGALAAWCYNKFYNISLPSYLGFFAGKRFVPIMMATCSFILA 183 A V+GIPTLQ GVFGG+I G LAAWCYN+F+ + LP +LGFF+GKRFV I A SF+L Sbjct: 109 AMVVGIPTLQMGVFGGLISGILAAWCYNRFHTLQLPEFLGFFSGKRFVAIAAAFLSFLLG 168 Query: 184 FPMAIIWPSIQGGLNAFSEGLLASNTGLAVFLFGFIKRLLIPFGLHHIFHAPFWFEFGSY 243 + +W IQ G++A S + N + F+FG ++R LIP GLHHI++ FW+ FG Y Sbjct: 169 LALPYVWQHIQAGIDALSVIVNGDNQAASTFIFGLVERALIPLGLHHIWYPSFWYSFGDY 228 Query: 244 KNAAGQIIHGDQRIFIEQIRD-------NVPLTAGKFMQGEFPVMMFGLPAAALAIYQTA 296 GQ+IHGDQ I+ + + + N AGKFMQGEFP+M+F LPAA LA+Y A Sbjct: 229 TTQTGQVIHGDQTIWFKMLEEGVKSFSSNTYQNAGKFMQGEFPLMLFALPAACLAMYHEA 288 Query: 297 KKENKKVVAGLMLSGALTSFLTGITEPLEFSFLFVAPLLFFIHAVLDGLSFLILYLLDLH 356 +NKK+ +G++ S ALT FLTGITEP+EF+F+FVAP+L+ +A++ GL+++ +YLLD H Sbjct: 289 STKNKKIASGILFSAALTCFLTGITEPVEFTFIFVAPVLYVFNAIMAGLAYMCMYLLDAH 348 Query: 357 LGYTFSGGFIDFFLLGILPN----KTQWWLVIPVGLVYAAIYYIIFRFLIVKFNFKTPGR 412 + +FS G ID+ GILP+ +T + + VG+ A IYY FRF+I +F+ KTPGR Sbjct: 349 IAKSFSAGLIDYISFGILPSFNGYQTHYLNAVIVGIPMAIIYYFTFRFVIRRFDVKTPGR 408 Query: 413 EDKEVKSSNVAASELPFKVLDAMGGKANIKHLDACITRLRVEVNDKAKVDVQELKDLGAS 472 D + + +EL ++ +GGK NI + ACITRLR+EV VD L LGA Sbjct: 409 VDVTASADDKTDAELAGNIVGLLGGKENITSVGACITRLRLEVARPDLVDKDGLNGLGAR 468 Query: 473 GVLEVGNN-MQAIFGPKSDQIKHDMQQIMDGK 503 GV+ VG+N +Q IFG ++ I + M GK Sbjct: 469 GVVFVGDNGIQVIFGARAQFIAQSLSG-MTGK 499 Lambda K H 0.324 0.143 0.421 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 901 Number of extensions: 48 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 675 Length of database: 499 Length adjustment: 36 Effective length of query: 639 Effective length of database: 463 Effective search space: 295857 Effective search space used: 295857 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (22.0 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory